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3:01
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U.S. Food and Drug Administration
FDA CDER Regulatory Science: Improving Drug Review with Data Standards
Data standards make the exchange of data predictable, consistent, and in a form that a scientific tool can use. Data standards help FDA make patient-centric decisions, integrating real-world data into the drug development process. Learn more about FDA’s Regulatory Science Program at https://www.fda.gov/Drugs/ScienceResearch/ucm294603.htm
4.3K views
Nov 16, 2017
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1.9K views · 18 shares | Ever wonder what it takes to take a drug from discovery to market? Dr. Theresa Strong discusses the stages of development and how you can help not only get drugs through clinical trials but also with the approval process. You can watch the entire presentation that includes information on each clinical trial here: https://www.fpwr.org/blog/2019-pws-clinical-trials-panel-video | The Foundation for Prader-Willi Research | Facebook
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